However, when we limited this to either novel variants or novel and nonynonymous variants, the affected children had more rare alleles than unaffected children in both categories (Table 6 ), but this difference did not reach statistical significance for either novel (p=0.112) or novel and nonsynonymous (p=0.097) when compared to the total number of variants passing QC among the affected and unaffected children.
1
0.1120
0.1120